Senior Biostatistician for Regulated Medical Devices

BD; Nebraska; Sur place; USD 110 000 - 176 000; Plein temps

Avantages offerts par ce poste

Health & Well-being benefits

401(k) retirement plan

Paid time off

Résumé du poste

BD seeks a Statistician/Biostatistician to support product development and clinical studies in a regulated healthcare environment. You will design studies, develop analysis plans, and communicate insights using R or SAS.

Master’s or PhD in Statistics/Biostatistics with 3+ years in regulated settings is required. You will collaborate across functions, manage multiple projects, and contribute to regulatory documentation and scientific communications.

Qualifications

• Master’s degree in Statistics, Biostatistics, or related field required or equivalent experience.
• 3+ years of experience in regulated healthcare, life sciences, or medical device environment.
• Experience applying statistical methods to product development, clinical research, or clinical trials.
• Proficiency in programming, documenting, and validating analyses using R and/or SAS.
• Experience leading cross-functional teams and managing multiple projects.
• Experience with technical report writing and presenting statistical findings.
• Familiarity with regulatory requirements and reproducible research practices.

Responsabilités

• Design, plan, analyze, and interpret studies to support product development and decision-making.
• Develop and review study protocols and regulatory documentation.
• Create and validate statistical code in R/SAS for data management and reporting.
• Prepare clear statistical reports for internal and external audiences.
• Present findings to cross-functional teams and contribute to publications.

Connaissances

Statistical analysis

Cross-functional collaboration

Communication

Problem solving

Regulatory awareness

Formation

Master's degree in Statistics/Biostatistics

PhD (preferred)

Outils

R

SAS

Description du poste

BD seeks a Statistician/Biostatistician to support product development and clinical studies in a regulated healthcare environment. You will design studies, develop analysis plans, and communicate insights using R or SAS.

Master’s or PhD in Statistics/Biostatistics with 3+ years in regulated settings is required. You will collaborate across functions, manage multiple projects, and contribute to regulatory documentation and scientific communications.